Clinical and genetic delineation of autosomal recessive and dominant ACTL6B-related developmental brain disorders.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Publication Year: 

Authors & Co-authors:  Cali Elisa E Quirin Tania T Rocca Clarissa C Efthymiou Stephanie S Riva Antonella A Marafi Dana D Zaki Maha S MS Suri Mohnish M Dominguez Roberto R Elbendary Hasnaa M HM

Event-based modeling in temporal lobe epilepsy demonstrates progressive atrophy from cross-sectional data.

Journal: Epilepsia

Publication Year: 2022

Authors & Co-authors:  Lopez Seymour M SM Aksman Leon M LM Oxtoby Neil P NP Vos Sjoerd B SB Rao Jun J Kaestner Erik E Alhusaini Saud S Alvim Marina M Bender Benjamin B Bernasconi Andrea A

Patterns of subregional cerebellar atrophy across epilepsy syndromes: An ENIGMA-Epilepsy study.

Journal: Epilepsia

Publication Year: 

Authors & Co-authors:  Kerestes Rebecca R Perry Andrew A Vivash Lucy L O'Brien Terence J TJ Alvim Marina K M MKM Arienzo Donatello D Aventurato Ítalo K ÍK Ballerini Alice A Baltazar Gabriel F GF Bargalló Núria N